Xiang Zhan, Ni Zhao, Anna Plantinga, Timothy A Thornton, Karen N Conneely, Michael P Epstein, Michael C Wu. Genetics 2017
Times Cited: 21
Times Cited: 21
Times Cited
Times Co-cited
Similarity
Rare-variant association testing for sequencing data with the sequence kernel association test.
Michael C Wu, Seunggeun Lee, Tianxi Cai, Yun Li, Michael Boehnke, Xihong Lin. Am J Hum Genet 2011
Michael C Wu, Seunggeun Lee, Tianxi Cai, Yun Li, Michael Boehnke, Xihong Lin. Am J Hum Genet 2011
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Rare-variant association analysis: study designs and statistical tests.
Seunggeung Lee, Gonçalo R Abecasis, Michael Boehnke, Xihong Lin. Am J Hum Genet 2014
Seunggeung Lee, Gonçalo R Abecasis, Michael Boehnke, Xihong Lin. Am J Hum Genet 2014
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Pleiotropy in complex traits: challenges and strategies.
Nadia Solovieff, Chris Cotsapas, Phil H Lee, Shaun M Purcell, Jordan W Smoller. Nat Rev Genet 2013
Nadia Solovieff, Chris Cotsapas, Phil H Lee, Shaun M Purcell, Jordan W Smoller. Nat Rev Genet 2013
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A Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants.
K Alaine Broadaway, David J Cutler, Richard Duncan, Jacob L Moore, Erin B Ware, Min A Jhun, Lawrence F Bielak, Wei Zhao, Jennifer A Smith, Patricia A Peyser,[...]. Am J Hum Genet 2016
K Alaine Broadaway, David J Cutler, Richard Duncan, Jacob L Moore, Erin B Ware, Min A Jhun, Lawrence F Bielak, Wei Zhao, Jennifer A Smith, Patricia A Peyser,[...]. Am J Hum Genet 2016
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Sequence Kernel Association Test of Multiple Continuous Phenotypes.
Baolin Wu, James S Pankow. Genet Epidemiol 2016
Baolin Wu, James S Pankow. Genet Epidemiol 2016
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A groupwise association test for rare mutations using a weighted sum statistic.
Bo Eskerod Madsen, Sharon R Browning. PLoS Genet 2009
Bo Eskerod Madsen, Sharon R Browning. PLoS Genet 2009
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Multi-SKAT: General framework to test for rare-variant association with multiple phenotypes.
Diptavo Dutta, Laura Scott, Michael Boehnke, Seunggeun Lee. Genet Epidemiol 2019
Diptavo Dutta, Laura Scott, Michael Boehnke, Seunggeun Lee. Genet Epidemiol 2019
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Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data.
Bingshan Li, Suzanne M Leal. Am J Hum Genet 2008
Bingshan Li, Suzanne M Leal. Am J Hum Genet 2008
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Multivariate phenotype association analysis by marker-set kernel machine regression.
Arnab Maity, Patrick F Sullivan, Jun-Ying Tzeng. Genet Epidemiol 2012
Arnab Maity, Patrick F Sullivan, Jun-Ying Tzeng. Genet Epidemiol 2012
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Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies.
Seunggeun Lee, Mary J Emond, Michael J Bamshad, Kathleen C Barnes, Mark J Rieder, Deborah A Nickerson, David C Christiani, Mark M Wurfel, Xihong Lin. Am J Hum Genet 2012
Seunggeun Lee, Mary J Emond, Michael J Bamshad, Kathleen C Barnes, Mark J Rieder, Deborah A Nickerson, David C Christiani, Mark M Wurfel, Xihong Lin. Am J Hum Genet 2012
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Multi-trait analysis of genome-wide association summary statistics using MTAG.
Patrick Turley, Raymond K Walters, Omeed Maghzian, Aysu Okbay, James J Lee, Mark Alan Fontana, Tuan Anh Nguyen-Viet, Robbee Wedow, Meghan Zacher, Nicholas A Furlotte,[...]. Nat Genet 2018
Patrick Turley, Raymond K Walters, Omeed Maghzian, Aysu Okbay, James J Lee, Mark Alan Fontana, Tuan Anh Nguyen-Viet, Robbee Wedow, Meghan Zacher, Nicholas A Furlotte,[...]. Nat Genet 2018
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Kernel machine SNP-set testing under multiple candidate kernels.
Michael C Wu, Arnab Maity, Seunggeun Lee, Elizabeth M Simmons, Quaker E Harmon, Xinyi Lin, Stephanie M Engel, Jeffrey J Molldrem, Paul M Armistead. Genet Epidemiol 2013
Michael C Wu, Arnab Maity, Seunggeun Lee, Elizabeth M Simmons, Quaker E Harmon, Xinyi Lin, Stephanie M Engel, Jeffrey J Molldrem, Paul M Armistead. Genet Epidemiol 2013
23
Rare variant association test with multiple phenotypes.
Selyeong Lee, Sungho Won, Young Jin Kim, Yongkang Kim, Bong-Jo Kim, Taesung Park. Genet Epidemiol 2017
Selyeong Lee, Sungho Won, Young Jin Kim, Yongkang Kim, Bong-Jo Kim, Taesung Park. Genet Epidemiol 2017
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A mixed-model approach for genome-wide association studies of correlated traits in structured populations.
Arthur Korte, Bjarni J Vilhjálmsson, Vincent Segura, Alexander Platt, Quan Long, Magnus Nordborg. Nat Genet 2012
Arthur Korte, Bjarni J Vilhjálmsson, Vincent Segura, Alexander Platt, Quan Long, Magnus Nordborg. Nat Genet 2012
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Methods for Analyzing Multivariate Phenotypes in Genetic Association Studies.
Qiong Yang, Yuanjia Wang. J Probab Stat 2012
Qiong Yang, Yuanjia Wang. J Probab Stat 2012
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Optimal tests for rare variant effects in sequencing association studies.
Seunggeun Lee, Michael C Wu, Xihong Lin. Biostatistics 2012
Seunggeun Lee, Michael C Wu, Xihong Lin. Biostatistics 2012
19
Efficient multivariate linear mixed model algorithms for genome-wide association studies.
Xiang Zhou, Matthew Stephens. Nat Methods 2014
Xiang Zhou, Matthew Stephens. Nat Methods 2014
19
Maximizing the power of principal-component analysis of correlated phenotypes in genome-wide association studies.
Hugues Aschard, Bjarni J Vilhjálmsson, Nicolas Greliche, Pierre-Emmanuel Morange, David-Alexandre Trégouët, Peter Kraft. Am J Hum Genet 2014
Hugues Aschard, Bjarni J Vilhjálmsson, Nicolas Greliche, Pierre-Emmanuel Morange, David-Alexandre Trégouët, Peter Kraft. Am J Hum Genet 2014
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A method for analyzing multiple continuous phenotypes in rare variant association studies allowing for flexible correlations in variant effects.
Jianping Sun, Karim Oualkacha, Vincenzo Forgetta, Hou-Feng Zheng, J Brent Richards, Antonio Ciampi, Celia Mt Greenwood. Eur J Hum Genet 2016
Jianping Sun, Karim Oualkacha, Vincenzo Forgetta, Hou-Feng Zheng, J Brent Richards, Antonio Ciampi, Celia Mt Greenwood. Eur J Hum Genet 2016
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Calibrating a coalescent simulation of human genome sequence variation.
Stephen F Schaffner, Catherine Foo, Stacey Gabriel, David Reich, Mark J Daly, David Altshuler. Genome Res 2005
Stephen F Schaffner, Catherine Foo, Stacey Gabriel, David Reich, Mark J Daly, David Altshuler. Genome Res 2005
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Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autism.
Iuliana Ionita-Laza, Marinela Capanu, Silvia De Rubeis, Kenneth McCallum, Joseph D Buxbaum. PLoS Genet 2014
Iuliana Ionita-Laza, Marinela Capanu, Silvia De Rubeis, Kenneth McCallum, Joseph D Buxbaum. PLoS Genet 2014
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Unified Sequence-Based Association Tests Allowing for Multiple Functional Annotations and Meta-analysis of Noncoding Variation in Metabochip Data.
Zihuai He, Bin Xu, Seunggeun Lee, Iuliana Ionita-Laza. Am J Hum Genet 2017
Zihuai He, Bin Xu, Seunggeun Lee, Iuliana Ionita-Laza. Am J Hum Genet 2017
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A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST).
Stephan Morgenthaler, William G Thilly. Mutat Res 2007
Stephan Morgenthaler, William G Thilly. Mutat Res 2007
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Meta-analysis of correlated traits via summary statistics from GWASs with an application in hypertension.
Xiaofeng Zhu, Tao Feng, Bamidele O Tayo, Jingjing Liang, J Hunter Young, Nora Franceschini, Jennifer A Smith, Lisa R Yanek, Yan V Sun, Todd L Edwards,[...]. Am J Hum Genet 2015
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MultiPhen: joint model of multiple phenotypes can increase discovery in GWAS.
Paul F O'Reilly, Clive J Hoggart, Yotsawat Pomyen, Federico C F Calboli, Paul Elliott, Marjo-Riitta Jarvelin, Lachlan J M Coin. PLoS One 2012
Paul F O'Reilly, Clive J Hoggart, Yotsawat Pomyen, Federico C F Calboli, Paul Elliott, Marjo-Riitta Jarvelin, Lachlan J M Coin. PLoS One 2012
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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, Nick Patterson, Mark J Daly, Alkes L Price, Benjamin M Neale. Nat Genet 2015
Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, Nick Patterson, Mark J Daly, Alkes L Price, Benjamin M Neale. Nat Genet 2015
14
USAT: A Unified Score-Based Association Test for Multiple Phenotype-Genotype Analysis.
Debashree Ray, James S Pankow, Saonli Basu. Genet Epidemiol 2016
Debashree Ray, James S Pankow, Saonli Basu. Genet Epidemiol 2016
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Abundant pleiotropy in human complex diseases and traits.
Shanya Sivakumaran, Felix Agakov, Evropi Theodoratou, James G Prendergast, Lina Zgaga, Teri Manolio, Igor Rudan, Paul McKeigue, James F Wilson, Harry Campbell. Am J Hum Genet 2011
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14
PSEA: Phenotype Set Enrichment Analysis--a new method for analysis of multiple phenotypes.
Janina S Ried, Angela Döring, Konrad Oexle, Christa Meisinger, Juliane Winkelmann, Norman Klopp, Thomas Meitinger, Annette Peters, Karsten Suhre, H-Erich Wichmann,[...]. Genet Epidemiol 2012
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Rare variant testing across methods and thresholds using the multi-kernel sequence kernel association test (MK-SKAT).
Eugene Urrutia, Seunggeun Lee, Arnab Maity, Ni Zhao, Judong Shen, Yun Li, Michael C Wu. Stat Interface 2015
Eugene Urrutia, Seunggeun Lee, Arnab Maity, Ni Zhao, Judong Shen, Yun Li, Michael C Wu. Stat Interface 2015
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PRIMe: a method for characterization and evaluation of pleiotropic regions from multiple genome-wide association studies.
Jie Huang, Andrew D Johnson, Christopher J O'Donnell. Bioinformatics 2011
Jie Huang, Andrew D Johnson, Christopher J O'Donnell. Bioinformatics 2011
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Associating Multivariate Quantitative Phenotypes with Genetic Variants in Family Samples with a Novel Kernel Machine Regression Method.
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Sequence kernel association test for quantitative traits in family samples.
Han Chen, James B Meigs, Josée Dupuis. Genet Epidemiol 2013
Han Chen, James B Meigs, Josée Dupuis. Genet Epidemiol 2013
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Testing for association with multiple traits in generalized estimation equations, with application to neuroimaging data.
Yiwei Zhang, Zhiyuan Xu, Xiaotong Shen, Wei Pan. Neuroimage 2014
Yiwei Zhang, Zhiyuan Xu, Xiaotong Shen, Wei Pan. Neuroimage 2014
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A powerful microbiome-based association test and a microbial taxa discovery framework for comprehensive association mapping.
Hyunwook Koh, Martin J Blaser, Huilin Li. Microbiome 2017
Hyunwook Koh, Martin J Blaser, Huilin Li. Microbiome 2017
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Powerful and Adaptive Testing for Multi-trait and Multi-SNP Associations with GWAS and Sequencing Data.
Junghi Kim, Yiwei Zhang, Wei Pan. Genetics 2016
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A Powerful Pathway-Based Adaptive Test for Genetic Association with Common or Rare Variants.
Wei Pan, Il-Youp Kwak, Peng Wei. Am J Hum Genet 2015
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Sequence kernel association tests for the combined effect of rare and common variants.
Iuliana Ionita-Laza, Seunggeun Lee, Vlad Makarov, Joseph D Buxbaum, Xihong Lin. Am J Hum Genet 2013
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Powerful SNP-set analysis for case-control genome-wide association studies.
Michael C Wu, Peter Kraft, Michael P Epstein, Deanne M Taylor, Stephen J Chanock, David J Hunter, Xihong Lin. Am J Hum Genet 2010
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Prioritizing individual genetic variants after kernel machine testing using variable selection.
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Statistical analysis strategies for association studies involving rare variants.
Vikas Bansal, Ondrej Libiger, Ali Torkamani, Nicholas J Schork. Nat Rev Genet 2010
Vikas Bansal, Ondrej Libiger, Ali Torkamani, Nicholas J Schork. Nat Rev Genet 2010
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Natural variations and genome-wide association studies in crop plants.
Xuehui Huang, Bin Han. Annu Rev Plant Biol 2014
Xuehui Huang, Bin Han. Annu Rev Plant Biol 2014
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Analyzing Association Mapping in Pedigree-Based GWAS Using a Penalized Multitrait Mixed Model.
Jin Liu, Can Yang, Xingjie Shi, Cong Li, Jian Huang, Hongyu Zhao, Shuangge Ma. Genet Epidemiol 2016
Jin Liu, Can Yang, Xingjie Shi, Cong Li, Jian Huang, Hongyu Zhao, Shuangge Ma. Genet Epidemiol 2016
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Multiple-trait genome-wide association study based on principal component analysis for residual covariance matrix.
H Gao, Y Wu, T Zhang, Y Wu, L Jiang, J Zhan, J Li, R Yang. Heredity (Edinb) 2014
H Gao, Y Wu, T Zhang, Y Wu, L Jiang, J Zhan, J Li, R Yang. Heredity (Edinb) 2014
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Genome-wide efficient mixed-model analysis for association studies.
Xiang Zhou, Matthew Stephens. Nat Genet 2012
Xiang Zhou, Matthew Stephens. Nat Genet 2012
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An efficient multi-locus mixed-model approach for genome-wide association studies in structured populations.
Vincent Segura, Bjarni J Vilhjálmsson, Alexander Platt, Arthur Korte, Ümit Seren, Quan Long, Magnus Nordborg. Nat Genet 2012
Vincent Segura, Bjarni J Vilhjálmsson, Alexander Platt, Arthur Korte, Ümit Seren, Quan Long, Magnus Nordborg. Nat Genet 2012
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SNP selection in genome-wide and candidate gene studies via penalized logistic regression.
Kristin L Ayers, Heather J Cordell. Genet Epidemiol 2010
Kristin L Ayers, Heather J Cordell. Genet Epidemiol 2010
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Methods for meta-analysis of multiple traits using GWAS summary statistics.
Debashree Ray, Michael Boehnke. Genet Epidemiol 2018
Debashree Ray, Michael Boehnke. Genet Epidemiol 2018
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An atlas of genetic correlations across human diseases and traits.
Brendan Bulik-Sullivan, Hilary K Finucane, Verneri Anttila, Alexander Gusev, Felix R Day, Po-Ru Loh, Laramie Duncan, John R B Perry, Nick Patterson, Elise B Robinson,[...]. Nat Genet 2015
Brendan Bulik-Sullivan, Hilary K Finucane, Verneri Anttila, Alexander Gusev, Felix R Day, Po-Ru Loh, Laramie Duncan, John R B Perry, Nick Patterson, Elise B Robinson,[...]. Nat Genet 2015
14
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.